ENST00000394867.9:n.1184G>C
|
|
|
ENST00000687128.1:n.1184G>C
|
|
|
ENST00000688002.1:n.1039G>C
|
|
|
ENST00000689792.1:n.649G>C
|
|
|
ENST00000262948.10:c.745G>C
MANE Select
|
ENSP00000262948.4:p.Asp249His
|
|
ENST00000262948.9:c.745G>C
|
ENSP00000262948.3:p.Asp249His
|
|
ENST00000394867.8:c.454G>C
|
ENSP00000378336.1:p.Asp152His
|
|
ENST00000593364.5:n.692G>C
|
|
|
ENST00000595715.1:n.560G>C
|
|
|
ENST00000597263.5:n.169+1644G>C
|
|
|
ENST00000599021.1:c.29+1644G>C
|
|
|
ENST00000600584.5:n.1305G>C
|
|
|
ENST00000601786.5:n.1046G>C
|
|
|
NM_030662.3:c.745G>C , LRG_750t1:c.745G>C
|
NP_109587.1:p.Asp249His
|
|
XM_006722799.2:c.705+1644G>C
|
XP_006722862.1:n.705+1644G>C
|
|
XM_011528133.1:c.175G>C
|
XP_011526435.1:p.Asp59His
|
|
XM_017026989.1:c.745G>C
|
XP_016882478.1:p.Asp249His
|
|
XM_017026990.1:c.705+1644G>C
|
XP_016882479.1:n.705+1644G>C
|
|
NM_030662.4:c.745G>C
MANE Select
|
NP_109587.1:p.Asp249His
|
|